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酵母的透射电子显微镜和免疫细胞化学研究:通过电子显微镜分析3-羟基-3-甲基戊二酰辅酶A还原酶的过量生产。

Transmission electron microscopy and immunocytochemical studies of yeast: analysis of HMG-CoA reductase overproduction by electron microscopy.

作者信息

Wright R, Rine J

机构信息

Department of Biochemistry, University of California, Berkeley 94720.

出版信息

Methods Cell Biol. 1989;31:473-512. doi: 10.1016/s0091-679x(08)61624-6.

Abstract

The results and anecdotes presented here are intended only as a general guide to other would-be immunocytochemists, because other proteins will undoubtedly respond at least somewhat differently than does HMG-CoA reductase. Nevertheless, based on these experiences, we offer the following suggestions: 1. Antiserum of high specificity should be raised and affinity-purified. Using this antiserum, immunofluorescence microscopy should be attempted before resorting to electron microscopic localization. In the absence of immunolocalization at the light-microscope level, it may be a waste of time to pursue the problem to higher levels of resolution. 2. Cells should be prefixed in 1% formaldehyde-1% glutaraldehyde. Direct fixation of the growing culture and use of phosphate buffer are recommended. The prefixed sample can then be divided into two or three aliquots. One aliquot should receive no postfixation (for optimal immunoreactivity), while the others can be postfixed in osmium-potassium ferricyanide (for possible immunolocalization) or permanganate (for ultrastructural analysis). Because of its ease of use, Spurr's resin should be tried initially. If immunocytochemistry is successful, no further preparations are necessary. If unsuccessful, LR White resin is recommended, but the sample must be treated to remove the cell wall. Electron microscopy and immunocytochemistry offer views into the molecular arrangement of individual cells, a view not easily obtained by other means. It is satisfying and often enlightening to be able to see the extremes as well as the average. In studies of the organization of karmellae, for example, ultrastructural analysis easily revealed the asymmetric segregation pattern, while immunoblots and cell fractionation could not even demonstrate the existence of this membrane organization. The richness of the information available to those who can avert reductionist tendencies, even for a short time, is remarkable.

摘要

本文所呈现的结果和轶事仅作为其他有志于从事免疫细胞化学研究人员的一般指南,因为其他蛋白质的反应无疑至少会与HMG - CoA还原酶有所不同。尽管如此,基于这些经验,我们提出以下建议:1. 应制备高特异性抗血清并进行亲和纯化。使用这种抗血清,在采用电子显微镜定位之前应尝试免疫荧光显微镜检查。如果在光学显微镜水平未实现免疫定位,将问题提升到更高分辨率水平可能是浪费时间。2. 细胞应先用1%甲醛 - 1%戊二醛固定。建议直接固定生长中的培养物并使用磷酸盐缓冲液。然后可将固定后的样品分成两到三份。一份不应进行后固定(以获得最佳免疫反应性),而其他份可分别用铁氰化钾锇(用于可能的免疫定位)或高锰酸盐(用于超微结构分析)进行后固定。由于其易于使用,应首先尝试Spurr树脂。如果免疫细胞化学成功,无需进一步制备。如果不成功,建议使用LR White树脂,但样品必须经过处理以去除细胞壁。电子显微镜和免疫细胞化学能够深入了解单个细胞的分子排列,这是其他方法不易获得的视角。能够看到极端情况以及平均值既令人满意又常常具有启发性。例如,在对卡氏菌组织的研究中,超微结构分析很容易揭示不对称分离模式,而免疫印迹和细胞分级分离甚至无法证明这种膜组织的存在。对于那些能够避免还原论倾向的人来说,哪怕只是短时间内,所获得信息的丰富程度也是惊人的。

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